Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A combination investigational therapy for chronic hepatitis C virus (HCV) infection, specifically genotype 1, composed of valopicitabine (NM283), an oral small molecule prodrug of 2'-C-methylcytidine that inhibits HCV RNA polymerase (NS5B), and peginterferon alfa-2b, a recombinant, pegylated interferon that stimulates the innate antiviral immune response via activation of the type 1 interferon receptor and subsequent JAK/STAT signaling. The combination was developed as an alternative for patients not responding to standard therapies, aiming to improve sustained virological response rates in both treatment-naive and treatment-experienced populations. Clinical trials showed marked reductions in viral load and a notable percentage of patients achieving undetectable HCV RNA, though some trials suggested efficacy was not superior to standard of care and ribavirin was absent in combination arms[1][3][5].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on valopicitabine + peginterferon alfa-2b.